Apoquel

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

oclacitinib maleate

Available from:

Zoetis Belgium SA

ATC code:

QD11AH90

INN (International Name):

oclacitinib maleate

Therapeutic group:

Klieb

Therapeutic area:

Aġenti għad-dermatite, esklużi kortikosterojdi

Therapeutic indications:

- Treatment of pruritus associated with allergic dermatitis in dogs. - Treatment of clinical manifestations of atopic dermatitis in dogs.

Product summary:

Revision: 8

Authorization status:

Awtorizzat

Authorization date:

2013-09-12

Patient Information leaflet

                                28
B. FULJETT TA’ TAGĦRIF
29
FULJETT TA’ TAGĦRIF:
APOQUEL 3.6 MG PILLOLI MIKSIJA B'RITA GĦAL KLIEB
APOQUEL
5.4 MG PILLOLI MIKSIJA B'RITA GĦAL KLIEB
APOQUEL 16 MG PILLOLI MIKSIJA B'RITA GĦAL KLIEB
1.
L-ISEM U L-INDIRIZZ TAD-DETENTUR TAL-AWTORIZZAZZJONI GĦAT-
TQEGĦID FIS-SUQ U TAD-DETENTUR TAL-AWTORIZZAZZJONI GĦALL-
MANIFATTURA RESPONSABBLI GĦALL-ĦRUĠ TAL-LOTT, JEKK DIFFERENTI
Detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
Zoetis Belgium SA
Rue Laid Burniat 1
1348 Louvain-la-Neuve
IL-BELGJU
Manifattur responsabbli għall-ħrug tal-lott:
Pfizer Italia S.R.L.
Via del Commercio 25/27
63100 Marino Del Tronto (AP)
L-ITALJA
jew
Zoetis Belgium SA
Rue Laid Burniat 1
1348 Louvain-la-Neuve
IL-BELGJU
2.
ISEM TAL-PRODOTT MEDIĊINALI VETERINARJU
Apoquel 3.6 mg pilloli miksija b'rita għal klieb
Apoquel
5.4 mg pilloli miksija b'rita għal klieb
Apoquel 16 mg pilloli miksija b'rita għal klieb
oclacitinib
3.
DIKJARAZZJONI TAS-SUSTANZA(I) ATTIVA(I) U INGREDJENT(I) OĦRA
Kull pillola miksija b’rita fiha 3.6 mg, 5.4 mg jew 16 mg
oclacitinib (bħala oclacitinib maleate).
Abjad għal abjad fl-isfar, pilloli miksija b'rita b’forma tawwalija
b’linja fejn taqsam fuq żewġ naħat u
mmarkati bl-ittri "AQ" u "S", "M" jew "L" fuq iż-żewġ naħat.
L-ittri "S", "M" u "L" jirreferu għall-
qawwiet differenti tal-pilloli: "S" huwa fuq il-pilloli 3.6 mg, "M"
fuq il-pilloli 5.4 mg, u "L" fuq il-
pilloli 16 mg.
Il-pilloli jistgħu jinqasmu f’nofsijiet indaqs.
4.
INDIKAZZJONI(JIET)
Trattament tal-ħakk assoċjat ma’ dermatite allerġika fil-klieb.
Trattament ta 'manifestazzjonijiet kliniċi ta' dermatite atopika
fil-klieb.
30
5.
KONTRAINDIKAZZJONIJIET
Tużax f'każ ta' sensittività għall-oclacitinib jew
għall-kwalunkwe ingredjent ieħor.
Tużax fi klieb ta’ età anqas minn 12-il xahar jew ta’ piż anqas
minn 3 kg.
Tużax fi klieb b’evindenza ta’ immunità mnaqqsa,
bħall-iperadrenokortiċiżmu, jew b'evidenza ta'
neoplasja progressiva malinna billi s-sustanza attiva ma ġietx
evalwata f'dawn il-każijiet.
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNESS I
KARATTERISTIĊI TAL-PRODOTT FIL-QOSOR
2
1.
ISEM TAL-PRODOTT MEDIĊINALI VETERINARJU
Apoquel 3.6 mg pilloli miksija b'rita għal klieb
Apoquel
5.4 mg pilloli miksija b'rita għal klieb
Apoquel 16 mg pilloli miksija b'rita għal klieb
2.
KOMPOŻIZZJONI KWALITATTIVA U KWANTITATTIVA
SUSTANZA ATTIVA:
Kull pillola miksija b'rita fiha:
Apoquel 3.6 mg:
3.6 mg oclacitinib (bħala oclacitinib maleate)
Apoquel 5.4 mg:
5.4 mg oclacitinib (bħala oclacitinib maleate)
Apoquel 16 mg:
16 mg oclacitinib (bħala oclacitinib maleate)
Għal-lista sħiħa tal-ingredjenti mhux attivi, ara s-sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Pilloli miksija b'rita.
Abjad għal abjad fl-isfar, pilloli miksija b'rita b’forma tawwalija
b’linja fejn taqsam fuq żewġ naħat u
mmarkati bl-ittri "AQ" u "S", "M" jew "L" fuq iż-żewġ naħat.
L-ittri "S", "M" u "L" jirreferu għall-
qawwiet differenti tal-pilloli: "S" huwa fuq il-pilloli 3.6 mg, "M"
fuq il-pilloli 5.4 mg, u "L" fuq il-
pilloli 16 mg.
Il-pilloli jistgħu jinqasmu f’nofsijiet indaqs.
4
TAGĦRIF KLINIKU
4.1
SPEĊI LI FUQHOM SER JINTUŻA L-PRODOTT
Klieb
4.2
INDIKAZZJONIJIET GĦAL UŻU TAL-PRODOTT LI JISPEĊIFIKAW L-ISPEĊI LI
FUQHOM SE JINTUŻA L-PRODOTT
Trattament tal-ħakk assoċjat ma’ dermatite allerġika fil-klieb.
Trattament ta' manifestazzjonijiet kliniċi ta' dermatite atopika
fil-klieb.
4.3
KONTRA-INDIKAZZJONIJIET
Tużax f'każ ta' sensittività għall-ingredjent attiv jew għal
ingredjenti oħra.
Tużax fi klieb ta’ età anqas minn 12-il xahar jew ta’ piż anqas
minn 3 kg.
Tużax fi klieb b’evindenza ta’ immunità mnaqqsa,
bħall-iperadrenokortiċiżmu, jew b'evidenza ta'
neoplasja progressiva malinna billi s-sustanza attiva ma ġietx
evalwata f'dawn il-każijiet.
4.4
TWISSIJIET SPEĊJALI GĦAL KULL SPEĊI LI GĦALIHA HU INDIKAT
IL-PRODOTT
Xejn.
3
4.5
PREKAWZJONIJIET SPEĊJALI GĦALL-UŻU
Prekawzjonijiet speċjali għall-użu fl-annimali:
Oclacitinib jimmodula s-sistema immunitarja u jista’ jżid
is-suxxettibbiltà għall-infezzjoni u jiggrava
kundizzjo
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 21-01-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 21-01-2022
Public Assessment Report Public Assessment Report Bulgarian 21-01-2022
Patient Information leaflet Patient Information leaflet Spanish 21-01-2022
Public Assessment Report Public Assessment Report Spanish 21-01-2022
Patient Information leaflet Patient Information leaflet Czech 21-01-2022
Public Assessment Report Public Assessment Report Czech 21-01-2022
Patient Information leaflet Patient Information leaflet Danish 21-01-2022
Public Assessment Report Public Assessment Report Danish 21-01-2022
Patient Information leaflet Patient Information leaflet German 21-01-2022
Public Assessment Report Public Assessment Report German 21-01-2022
Patient Information leaflet Patient Information leaflet Estonian 21-01-2022
Public Assessment Report Public Assessment Report Estonian 21-01-2022
Patient Information leaflet Patient Information leaflet Greek 21-01-2022
Public Assessment Report Public Assessment Report Greek 21-01-2022
Patient Information leaflet Patient Information leaflet English 21-01-2022
Public Assessment Report Public Assessment Report English 21-01-2022
Patient Information leaflet Patient Information leaflet French 21-01-2022
Public Assessment Report Public Assessment Report French 21-01-2022
Patient Information leaflet Patient Information leaflet Italian 21-01-2022
Public Assessment Report Public Assessment Report Italian 21-01-2022
Patient Information leaflet Patient Information leaflet Latvian 21-01-2022
Public Assessment Report Public Assessment Report Latvian 21-01-2022
Patient Information leaflet Patient Information leaflet Lithuanian 21-01-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 21-01-2022
Public Assessment Report Public Assessment Report Lithuanian 21-01-2022
Patient Information leaflet Patient Information leaflet Hungarian 21-01-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 21-01-2022
Public Assessment Report Public Assessment Report Hungarian 21-01-2022
Patient Information leaflet Patient Information leaflet Dutch 21-01-2022
Public Assessment Report Public Assessment Report Dutch 21-01-2022
Patient Information leaflet Patient Information leaflet Polish 21-01-2022
Public Assessment Report Public Assessment Report Polish 21-01-2022
Patient Information leaflet Patient Information leaflet Portuguese 21-01-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 21-01-2022
Public Assessment Report Public Assessment Report Portuguese 21-01-2022
Patient Information leaflet Patient Information leaflet Romanian 21-01-2022
Public Assessment Report Public Assessment Report Romanian 21-01-2022
Patient Information leaflet Patient Information leaflet Slovak 21-01-2022
Public Assessment Report Public Assessment Report Slovak 21-01-2022
Patient Information leaflet Patient Information leaflet Slovenian 21-01-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 21-01-2022
Public Assessment Report Public Assessment Report Slovenian 21-01-2022
Patient Information leaflet Patient Information leaflet Finnish 21-01-2022
Public Assessment Report Public Assessment Report Finnish 21-01-2022
Patient Information leaflet Patient Information leaflet Swedish 21-01-2022
Public Assessment Report Public Assessment Report Swedish 21-01-2022
Patient Information leaflet Patient Information leaflet Norwegian 21-01-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 21-01-2022
Patient Information leaflet Patient Information leaflet Icelandic 21-01-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 21-01-2022
Patient Information leaflet Patient Information leaflet Croatian 21-01-2022
Public Assessment Report Public Assessment Report Croatian 21-01-2022

Search alerts related to this product

View documents history